Source: BEFREE

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11 		potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C0432217
Disease: Wolcott-Rallison syndrome
Wolcott-Rallison syndrome 		disease 0.010 None < 0.001 1 0 2014 2014
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11 		potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C0851578
Disease: Sleep Disorders
Sleep Disorders 		group 0.010 None 1.000 1 0 2017 2017
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11 		potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		group 0.010 None 1.000 1 0 2018 2018
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11 		potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C0037317
Disease: Sleep disturbances
Sleep disturbances 		phenotype 0.010 None 1.000 1 0 2017 2017
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11 		potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C0221005
Disease: Mauriac's syndrome
Mauriac's syndrome 		disease 0.010 None 1.000 1 1 2016 2016
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11 		potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C0947785
Disease: [D]Sleep disturbances (& [hypersomnia] or [insomnia])
[D]Sleep disturbances (& [hypersomnia] or [insomnia]) 		phenotype 0.010 None 1.000 1 0 2017 2017
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11 		potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C0023976
Disease: Long QT Syndrome
Long QT Syndrome 		disease 0.010 None 1.000 1 0 2001 2001
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11 		potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C0022735
Disease: Klinefelter Syndrome
Klinefelter Syndrome 		disease 0.010 None 1.000 1 0 2018 2018
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11 		potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C0022660
Disease: Kidney Failure, Acute
Kidney Failure, Acute 		disease 0.010 None 1.000 1 0 2014 2014
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11 		potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		disease 0.010 None 1.000 1 0 2017 2017
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11 		potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C0085612
Disease: Ventricular arrhythmia
Ventricular arrhythmia 		disease 0.010 None 1.000 1 0 2017 2017
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11 		potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction 		disease 0.010 None 1.000 1 0 2004 2004
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11 		potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C0432474
Disease: Klinefelter's syndrome - male with more than two X chromosomes
Klinefelter's syndrome - male with more than two X chromosomes 		disease 0.010 None 1.000 1 0 2018 2018
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11 		potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C0271680
Disease: Diabetic Polyneuropathies
Diabetic Polyneuropathies 		group 0.010 None 1.000 1 1 2017 2017
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11 		potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma 		disease 0.010 None 1.000 1 1 2014 2014
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11 		potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C0235162
Disease: Difficulty sleeping
Difficulty sleeping 		phenotype 0.010 None 1.000 1 0 2017 2017
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11 		potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C0235031
Disease: Neurologic Symptoms
Neurologic Symptoms 		group 0.010 None 1.000 1 0 2012 2012
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11 		potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C0233794
Disease: Memory impairment
Memory impairment 		phenotype 0.010 None 1.000 1 0 2019 2019
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11 		potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior 		phenotype 0.010 None 1.000 1 0 2016 2016
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11 		potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C0178874
Disease: Tumor Progression
Tumor Progression 		phenotype 0.010 None 1.000 1 0 2018 2018
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11 		potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C0745153
Disease: Hypoglycaemic episode
Hypoglycaemic episode 		disease 0.010 None 1.000 1 1 2017 2017
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11 		potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C1504532
Disease: Post transplant diabetes mellitus
Post transplant diabetes mellitus 		disease 0.010 None < 0.001 1 0 2017 2017
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11 		potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases 		group 0.010 None 1.000 1 2 2009 2009
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11 		potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		disease 0.010 None 1.000 1 1 2009 2009
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11 		potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		group 0.010 None 1.000 1 0 2007 2007